An alkylphenol copolymer, such as for use in a petroleum composition, is provided. The alkylphenol copolymer has at least the following repeating unit (I): ##STR00001## wherein: A is a direct bond or an alkylene; X is —C(O)O—, —OC(O)—, —C(O)N(R.sub.6)—, —N(R.sub.6)C(O)—, —C(O)—, —N(R.sub.6)—, —O—, or —S—; R.sub.6 is H or an alkyl; R.sub.1 includes a C.sub.1-C.sub.80 alkyl, a C.sub.2-C.sub.20 alkenyl, a C.sub.2-C.sub.20 alkynyl, a C.sub.3-C.sub.12 aryl, or a polyether; and n is an integer from 1 to 200. The present invention also provides a method for forming the alkylphenol copolymer containing the aforementioned repeating unit (I) as well as a method for forming a monomer for forming repeating unit (I).

Chemically inert, mechanically tough, cationic metallo-polyelectrolytes designed as durable anion-exchange membranes (AEMs) via ring-opening metathesis polymerization (ROMP) of cobaltocenium-containing cyclooctene with triazole as the only linker group, followed by backbone hydrogenation to provide a new class of AEMs with a polyethylene-like framework and alkaline-stable cobaltocenium cation for ion transport, which exhibit excellent thermal, chemical and mechanical stability, as well as high ion conductivity.

The present disclosure presents a disulfide containing monomer, its reduced form, its derivative, the synthesis method of this disulfide containing monomer, and the polymer containing the monomers disclosed thereof

A polymer blend, including at least one organic semiconductor (OSC) polymer, such that: the at least one OSC polymer is a diketopyrrolopyrrole-fused thiophene polymeric material, the fused thiophene is beta-substituted, the at least one OSC polymer has a first portion and a second portion, and at least one of the first portion or the second portion includes at least one UV-curable side chain.

Described herein are compositions and methods for processing photopolymers based on olefin metathesis. The compositions and methods comprise latent ruthenium complexes and photoacids and/or photoacid generators.

A method for manufacturing an electrolytic capacitor is provided. A conductive polymer solution is applied onto a porous main body. The porous main body includes a porous electrode body having an electrode material and a dielectric layer covering an outer surface of the electrode material. The conductive polymer solution contains conductive polymer particles whose average particle size ranges from 0.5 nm to 50 nm. A solid electrolyte is formed to completely or partially cover a surface of the dielectric layer. A material of the conductive polymer particles includes at least one of polythiophene having at least one sulfonic acid group and polyselenophene having at least one sulfonic acid group. An electrical conductivity of a dry membrane formed from the conductive polymer particles is higher than 25 S/cm. An amount of metal cations in the conductive polymer solution is less than 500 mg/kg.

A liquid composition includes a thiophene polymer; and at least one polymerization component selected from the group including a monomer and an oligomer.

A ring-opened copolymer composition has a ring-opened copolymer containing structural unit derived from a norbornene compound represented by general formula (1) below and structural unit derived from a monocyclic olefin, wherein a content of a norbornene compound represented by general formula (1) is 1 ppm by weight or more and 1000 ppm by weight or less based on the ring-opened copolymer, ##STR00001## wherein R.sup.1 to R.sup.4 are each a hydrogen atom, a hydrocarbon group having 1 to 20 carbon atoms, or a substituent containing a halogen atom, a silicon atom, an oxygen atom or a nitrogen atom, and R.sup.2 and R.sup.3 may be bonded to each other to form a ring, and “m” is 0 or 1.

This is to provide a non-halogen containing compound excellent in proton conductivity and capable of suitably being used for a polymer electrolytic fuel cell The compound of the present invention has a structure represented by the following general formula (I). ##STR00001## (In the above-mentioned general formula (I), “l” and “n” are molar fractions when l+n=1.0, and 0≤l<1.0 and 0<n≤1.0, A represents a structure represented by the following general formula (II) or (III), B represents a structure represented by the following general formula (VII), the respective structural units are random copolymerized, and at least one benzene ring in the formula (I) has at least one sulfo group.) ##STR00002## (In the above-mentioned general formula (II) or (III), R.sup.1 to R.sup.4 are each independently selected from hydrogen and an alkyl group having 1 to 3 carbon atoms, le and R.sup.2 form together with the carbon atom, they are attached to, an aromatic ring or a fused aromatic ring and R.sup.3 and R.sup.4 form together with the carbon atom, they are attached to, an aromatic ring or a fused aromatic ring, or R.sup.1, R.sup.3 and R.sup.4 are hydrogens and R.sup.2 is a single bond and bonded to the carbon of “c”, X is a single bond, or a structure represented by the following formula (IV), the following formula (V) or the following formula (VI), when X is a single bond, bonds “a”s are both bonded at ortho positions or both bonded at meta positions relative to the carbons bonded to X, when X is a structure represented by the following formula (IV), bonds “a”s are both bonded at para positions relative to the carbons bonded to X, and when it is a structure represented by the following formula (V), bonds “a”s are both bonded at para positions or both bonded at meta positions relative to the carbons bonded to x, when X is a structure represented by the following formula (VI), the bonds “a”s in the above-mentioned general formula (II) or (III) exist only one of these, and A binds to other structure or a structural unit by one of the bonds “a”s and the bond “b”.) ##STR00003##

A random copolymer comprising the monomer units A, B and C. In this random copolymer A comprises ##STR00001##
B comprises ##STR00002##
and C comprises an aryl group. Additionally, R1, R2, R3 and R4 are side chains independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, alkylthio, ester, ketone and aryl groups. X1 and X2 are independently selected from the group consisting of: H, Cl, F, CN, alkyl, alkoxy, ester, ketone, amide and aryl groups.